FDA 510(k) Application Details - K110409

Device Classification Name	Apparatus, Suction, Patient Care   More FDA Info for this Device
510(K) Number	K110409
Device Name	Apparatus, Suction, Patient Care
Applicant	C.R. BARD, INC. 605 NORTH 5600 WEST SALT LAKE CITY, UT 84116 US Other 510(k) Applications for this Company
Contact	HENRY BOLAND Other 510(k) Applications for this Contact
Regulation Number	870.5050   More FDA Info for this Regulation Number
Classification Product Code	DWM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/14/2011
Decision Date	05/11/2011
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review